Ferdinandusse, S., te Brinke, H., Ruiter, J. P., Haasjes, J., Oostheim, W., van Lenthe, H., . . . Waterham, H. R. (2019). A mutation creating an upstream translation initiation codon in SLC22A5 5′UTR is a frequent cause of primary carnitine deficiency. Hum Mutat.
Stile di citazione ChicagoFerdinandusse, Sacha, et al. "A Mutation Creating an Upstream Translation Initiation Codon in SLC22A5 5′UTR Is a Frequent Cause of Primary Carnitine Deficiency." Hum Mutat 2019.
Citazione MLAFerdinandusse, Sacha, et al. "A Mutation Creating an Upstream Translation Initiation Codon in SLC22A5 5′UTR Is a Frequent Cause of Primary Carnitine Deficiency." Hum Mutat 2019.
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